2-(Trichlorosilyl)ethyl acetate

Base Information

• Chemical Name: 2-(Trichlorosilyl)ethyl acetate
• CAS No.: 18204-80-3
• Molecular Formula: C4H7Cl3O2Si
• Molecular Weight: 221.543
• Hs Code.: 2931900090
• European Community (EC) Number: 242-092-7
• DSSTox Substance ID: DTXSID60885017
• Nikkaji Number: J266.056C
• Wikidata: Q82863650
• Mol file: 18204-80-3.mol

Synonyms:18204-80-3;2-(Trichlorosilyl)ethyl acetate;2-ACETOXYETHYLTRICHLOROSILANE;Acetoxyethyltrichlorosilane;2-trichlorosilylethyl acetate;Ethanol, 2-(trichlorosilyl)-, 1-acetate;Acetoxyethyl trichlorosilane;Ethanol, 2-(trichlorosilyl)-, acetate;2-Acetoxyethyl Trichlorosilane;EINECS 242-092-7;2-acetoxyethyl-trichlorosilane;SCHEMBL523168;DTXSID60885017;2-(Trichlorosilyl)ethanol acetate;MFCD00039289;FT-0637664;S00017;A847349

Chemical Property of 2-(Trichlorosilyl)ethyl acetate

Chemical Property:

• Refractive Index: 1.4427
• Boiling Point: 195.8 °C at 760 mmHg
• Flash Point: 72.2 °C
• PSA: 26.30000
• Density: 1.319 g/cm³
• LogP: 2.20480
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 219.928089
• Heavy Atom Count: 10
• Complexity: 122

Purity/Quality:

97% ^*data from raw suppliers

2-ACETOXYETHYLTRICHLOROSILANE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): C
• Hazard Codes: C
• Statements: 34-14
• Safety Statements: 26-36/37/39-45-27

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)OCC[Si](Cl)(Cl)Cl
• General Description: 2-Acetoxyethyltrichlorosilane is a silane compound characterized by the presence of an acetoxyethyl group and three chloro substituents attached to a silicon atom. It is used as a reagent in organic synthesis and surface modification due to its ability to form stable bonds with various substrates, particularly in the preparation of functionalized surfaces or as a precursor for further chemical transformations. 2-ACETOXYETHYLTRICHLOROSILANE is also known by alternative names such as Ethanol,2-(trichlorosilyl)-, acetate and (2-Acetoxyethyl)trichlorosilane. Its reactivity is primarily attributed to the trichlorosilyl group, which readily undergoes hydrolysis and condensation reactions.

Technology Process of 2-(Trichlorosilyl)ethyl acetate

There total 2 articles about 2-(Trichlorosilyl)ethyl acetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

vinyl acetate (108-05-4,9003-20-7) → (acetoxyethyl)trichlorosilane (18204-80-3)

Guidance literature:

With platinum on activated charcoal; trichlorosilane;

DOI:10.1021/ja01569a023

Reference yield:

→ (acetoxyethyl)trichlorosilane (18204-80-3)

Guidance literature:

Vinylacetat, Cl3SiH;

DOI:10.1007/BF00920862

Reference yield: 66.0%

sodium-bond phenylsilsesquioxane + (acetoxyethyl)trichlorosilane (18204-80-3) → acetoxyethyl-heptaphenyloctasilsesquioxane (757198-90-6)

Guidance literature:

With triethylamine; In tetrahydrofuran; at 20 ℃; for 2h;

DOI:10.1021/ma048877w

upstream raw materials:

vinyl acetate

Downstream raw materials:

acetoxyethyl-heptaphenyloctasilsesquioxane